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  1. Molecular Pathology and Genetics of Alport Syndrome (Contributions to Nephrology)
  2. Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  3. Gale Encyclopedia of Medicine: Alport syndrome by Carol A. Turkington, 2002-01-01
  4. The Molecular Genetics of X-Linked Alport Syndrome (Acta Biomedica Lovaniensia) by Caiying Guo, 1995-11
  5. Alport Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Carol Turkington, 2006
  6. Hereditary nephropathy with hearing loss: "Alport's syndrome" (Acta paediatrica Scandinavica : Supplement) by Ulla Marianne Iversen, 1974
  7. Hereditary hearing loss with nephropathy (Alport's syndrome); (Acta oto-laryngologica. Supplement[um]) by John Sidney Turner, 1970
  8. Familial nephritis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Maria, PhD Basile, 2005

41. Alport Syndrome
Health Search Engine, alport syndrome, Welcome to Medifocus! alport syndrome. Site Map Privacy Contact Advertise Health Directory Copyright 20002004.
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      Directory   Home: Health: Conditions and Diseases: Urological Disorders: Glomerular: Alport Syndrome (6) Pediatric Database - A definition of alport syndrome followed by clinical features, investigation and management. A Healthy Me - A detailed look at alport syndrome and its causes, symptoms, diagnosis, treatment and prevention. Iafrica Ask the Doctor - A mother asks for and receives general information about alport syndrome Alport Syndrome - Extensive data base for this disease along with message board, chat and resources. Mylifepath - In depth look at alport syndrome
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42. Alport Syndrome
Pediatric Database A definition of alport syndrome followed by clinical features, investigation and management. A Healthy Me - A
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Directory Home Health Conditions and Diseases Urological Disorders ... Glomerular : Alport Syndrome (6)
    Pediatric Database - A definition of alport syndrome followed by clinical features, investigation and management. A Healthy Me - A detailed look at alport syndrome and its causes, symptoms, diagnosis, treatment and prevention. Iafrica Ask the Doctor - A mother asks for and receives general information about alport syndrome. Alport Syndrome - Extensive data base for this disease along with message board, chat and resources. Mylifepath - In depth look at alport syndrome including a definition, description, causes and symptoms, diagnosis, treatment, prognosis, prevention, key terms and further reading. Alport Syndrome - Information about this hereditary renal disease. German site with English translation.

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43. Alport Syndrome Medical Definition Of Alport Syndrome In The Medical Dictionary.
Definition of alport syndrome in the Medical Dictionary and Thesaurus. Alport lookup. Provides search by definition of alport syndrome.
http://medical-dictionary.thefreedictionary.com/Alport syndrome
Dictionaries: General Computing Medical Legal Encyclopedia
Alport syndrome
Word: Word Starts with Ends with Definition Pronunciation: (AL-port SIN-drome) An inherited condition that results in kidney disease. It generally develops during early childhood and is more serious in boys than in girls. The condition can lead to end-stage renal disease, as well as hearing and vision problems. The common symptoms of this condition are chronic blood and protein in the urine.
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44. Alport Syndrome
alport syndrome. Disorders, Inc. Important It is possible that the main title of the report alport syndrome is not the name you expected.
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45. Alport Syndrome - Patient UK
alport syndrome Patient UK. A directory of UK health, disease, illness and related medical websites that provide patient information. alport syndrome.
http://www.patient.co.uk/alport_syndrome.htm
Alport Syndrome
UK sources of information and / or support
EdRenINFO
Information provided by the Royal Infirmary of Edinburgh Renal Unit for patients and for doctors who are not renal specialists. This site includes information about many kidney problems including Alport Syndrome.
Further sources / More detailed information
Some non-UK sites
The following list popular non-UK health information sites, mainly from the US. They have not been checked to see if Alport Syndrome is included but these large sites are comprehensive.
Evidence Based Medicine
For sites and information on Evidence Based Medicine.

46. CCHS Clinical Digital Library
alport syndrome Clinical Resources. Miscellaneous alport syndrome Clinical Resources Health Reviews for Primary Care Providers on the Internet Homepage
http://cchs-dl.slis.ua.edu/clinical/nephrology/glomerulonephritis/multisystem/al
Clinical Resources by Topic: Nephrology
Alport Syndrome Clinical Resources
Pediatrics Atlases Pathology Genetics ... Miscellaneous Resources See also:

47. CCHS Clinical Digital Library
alport syndrome Patient/Family Resources. Spanish Miscellaneous. Miscellaneous alport syndrome Patients/Family Resources Healthfinder (US DHHS) Homepage
http://cchs-dl.slis.ua.edu/patientinfo/nephrology/glomerulonephritis/multi/alpor
Patient/Family Resources by Topic: Nephrology
Alport Syndrome Patient/Family Resources
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48. Alport Syndrome
alport syndrome. Alport Alport. Because of the way alport syndrome is inherited, the disease tends to be more severe in men than in women.
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Alport Syndrome
Alport Syndrome is an inherited disease that affects the glomeruli, the tiny blood vessels within the kidneys that filter the blood of its wastes. It was first described by an English doctor, A. Cecil Alport. Because of the way Alport Syndrome is inherited, the disease tends to be more severe in men than in women. The central feature of the disease is the presence of blood in the urine. Boys with Alport Syndrome develop this symptom in infancy, while girls who carry the Alport gene may or may not have it. Another important symptom of Alport Syndrome is hearing loss. In boys with the disease, hearing loss is usually detectable by 8-10 years of age, and it may be severe enough to require the use of hearing aids. Hearing loss in girls tends to be much milder, rarely resulting in the need for hearing aids. Some boys with Alport Syndrome lose large amounts of protein in the urine, resulting in retention of fluid and body swelling. This condition is called "the nephrotic syndrome." With the passage of years, boys with Alport Syndrome develop the typical signs and symptoms of kidney failurehigh blood pressure, swelling, and in some cases, impaired growth. Some people with Alport Syndrome have an eye problem called anterior lenticonus, in which the shape of the lens becomes distorted. This can interfere with the sharpness of vision.

49. The National Kidney Foundation Of Illinois - JUST THE FACTS
about alport syndrome. What is alport syndrome? Because of the way alport syndrome is inherited, the disease tends to be more severe in men than in women.
http://www.nkfi.org/factsheets/Alport2.html
National Kidney Foundation of Illinois, Inc. connecting you to
JUST THE FACTS...
about
ALPORT SYNDROME
What is Alport Syndrome? What are its symptoms?
Alport Syndrome is an inherited disease that affects the glomeruli, the tiny blood vessels within the kidneys that filter the blood of its wastes. An English doctor, A. Cecil Alport, described many of the important features of the disease in the British Medical Journal in 1927, and his name has been associated with the disorder ever since.
Because of the way Alport Syndrome is inherited, the disease tends to be more severe in men than in women. The central feature of the disease is the presence of blood in the urine. Boys with Alport Syndrome develop this symptom in infancy, while girls who carry the Alport gene may or may not have it.
Another important symptom of Alport Syndrome is hearing loss. In boys with the disease, hearing loss is usually detectable by 8-10 years of age, and it may be severe enough to require the use of hearing aids. Hearing loss in girls tends to be much milder, rarely resulting in the need for hearing aids.
Some boys with Alport Syndrome lose large amounts of protein in the urine, resulting in retention of fluid and body swelling. This condition is called the "nephrotic syndrome." With the passage of years, boys with Alport Syndrome develop the typical signs and symptoms of kidney failurehigh blood pressure, swelling, and in some cases, impaired growth.

50. Disease Directory : Urological Disorders : Glomerular : Alport Syndrome
A Healthy Me A detailed look at alport syndrome and its causes, symptoms, diagnosis, treatment and prevention. alport syndrome - alport syndrome. Definition.
http://www.diseasedirectory.net/Urological_Disorders/Glomerular/Alport_Syndrome/
Wednesday, June 02, 2004 Urological Disorders Glomerular
Alport Syndrome

Glomerulonephritis
... Glomerular : Alport Syndrome
  • A Healthy Me - A detailed look at alport syndrome and its causes, symptoms, diagnosis, treatment and prevention. Alport Syndrome - Extensive data base for this disease along with message board, chat and resources. Alport syndrome - Alport syndrome. Definition. Description. Alport syndrome affects about one in 5,000 Americans, striking men more often and severely than women. Alport syndrome - Alport syndrome. Definition: Alport Causes, incidence, and risk factors: Alport syndrome is very similar to hereditary nephritis. There ALPORT SYNDROME - Alport Syndrome Because of the way Alport Syndrome is inherited, the disease tends to be more severe in men than in women. What are the symptoms? Alport syndrome Alport syndrome - MAIN SEARCH INDEX. Alport syndrome. Description. Alport syndrome affects about one in 5,000 Americans, striking men more often and severely than women. Alport Syndrome Clinical Resources - Alport Syndrome Clinical Resources. Miscellaneous Alport Syndrome Clinical Resources: Health Reviews for Primary Care Providers on the Internet: Homepage: Alport Syndrome Information - home > urological disorders > glomerular > alport syndrome Alport Syndrome. University of Newcastle-upon-Tyne Medical Dictionary: "Alport syndrome".

51. Alport Syndrome
alport syndrome. Alternative Names Causes, incidence, and risk factors alport syndrome is very similar to hereditary nephritis.
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52. Gale Encyclopedia Of Medicine Alport Syndrome
. alport syndrome affects about one in 5,000 Americans, striking men more often and severely than women....... alport syndrome.
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Alport syndrome
by Carol A. Turkington
Definition
A hereditary disease of the kidneys that primarily affects men, causing blood in the urine, hearing loss and eye problems. Eventually, kidney dialysis or transplant may be necessary.
Description
Alport syndrome affects about one in 5,000 Americans, striking men more often and severely than women. There are several varieties of the syndrome, some occurring in childhood and others not causing symptoms until men reach their 20s or 30s. All varieties of the syndrome are characterized by kidney disease that usually progresses to chronic kidney failure and by uremia (the presence of excessive amounts of urea and other waste products in the blood).
Alport syndrome in most cases is caused by a defect in one or more genes located on the X chromosome. It is usually inherited from the mother, who is a normal carrier. However, in up to 20% of cases there is no family history of the disorder. In these cases, there appears to be a spontaneous genetic mutation causing Alport syndrome.

53. Disease - Alport Syndrome - Hartford, Connecticut , Saint Francis Care
Disease alport syndrome - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart disease
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Disease - Alport syndrome
Male urinary system Definition: Alport syndrome is an inherited (usually X-linked) disorder involving damage to the kidney, blood in the urine , and in some families, loss of hearing . The disorder may also include eye defects Alternative Names: Hereditary nephritis; Hematuria - nephropathy - deafness; Hemorrhagic familial nephritis; Hereditary deafness and nephropathy Causes And Risk: Alport syndrome is very similar to hereditary nephritis. There may be nerve deafness and congenital eye abnormalities associated with Alport syndrome. The cause is a mutation in a gene for collagen. The disorder is uncommon, and most often affects males since the genetic defect is typically found on the X chromosome.
In women, the disorder is usually mild, with minimal or no symptoms. Women can transmit the gene for the disorder to their children, even if the woman has no symptoms of the disorder. In men, the symptoms are more severe and progress faster.
The disorder causes chronic glomerulonephritis with destruction of the glomeruli. Initially, there are no symptoms. Progressive destruction of the glomeruli causes

54. University Of Miami School Of Medicine - Glossary - Alport Syndrome
alport syndrome. alport syndrome An hereditary condition characterized by kidney disease, sensorineural (nerve) deafness and sometimes eye defects.
http://www.med.miami.edu/patients/glossary/art.asp?articlekey=10745

55. Alport Syndrome From Linkspider UK Health Directory
alport syndrome by Linkspider UK, alport syndrome links and alport syndrome topics from our Health directory. Helping you find what
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    Alport's Syndrome: Treatments
    Get the facts to make informed decisions about Alport's Syndrome. Our trustworthy Guide includes comprehensive information about standard of care,treatment options,latest advances.($19.95)

56. Alport Syndrome,Hereditary Nephritis,Alport Syndrome,Hereditary Nephritis,Heredi
alport syndrome,Hereditary Nephritis,alport syndrome,Hereditary Nephritis,Hereditary Nephritis and Nerve Deafness,Hereditary Nephropathy and Deafness.
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Alport Syndrome,Hereditary Nephritis,alport yndrome,hereditary nephritis,Alport Syndrome,Hereditary Nephritis,Hereditary Nephritis and Nerve Deafness,Hereditary Nephropathy and Deafness
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DISORDERS GLOSSARY Alport Syndrome
also known as:
Hereditary Nephritis
Nephritis and Nerve Deafness, Hereditary
Nephropathy and Deafness, Hereditary
Disorder Subdivisions
Alport Syndrome, Type I Alport Syndrome Type II Alport Syndrome, Type III Alport Syndrome, Type IV Alport Syndrome, Type V Epstein Syndrome (Type V) Alport Syndrome, Type VI (as defined by the National Organization for Rare Disorders
Alport Syndrome is a group of hereditary kidney disorders characterized by progressive deterioration of the glomerular basement membranes (GBMs), which are microscopic parts of the kidney. This deterioration may lead to chronic renal (kidney) failure causing excess waste products in the blood (uremia). Eventually severe renal failure (end-stage renal disease or ESRD) may develop.

57. Medical Encyclopedia
Back to main Health Information page Disease alport syndrome. Causes And Risk alport syndrome is very similar to hereditary nephritis.
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58. Urological Disorders, Glomerular, Alport Syndrome
More alport syndrome Categories » Submit Your Site to the alport syndrome category. Submit Your Site to the alport syndrome category. Health Spotlight.
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  • A Healthy Me - A detailed look at alport syndrome and its causes, symptoms, diagnosis, treatment and prevention.
  • Alport Syndrome - Information about this hereditary renal disease. German site with English translation.
  • Alport Syndrome - Extensive data base for this disease along with message board, chat and resources.
  • Iafrica Ask the Doctor - A mother asks for and receives general information about alport syndrome.
  • Mylifepath - In depth look at alport syndrome including a definition, description, causes and symptoms, diagnosis, treatment, prognosis, prevention, key terms and further reading.
  • Pediatric Database - A definition of alport syndrome followed by clinical features, investigation and management.

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59. Medical Encyclopedia
BACK, Back to main Health Information page Disease alport syndrome. Causes And Risk alport syndrome is very similar to hereditary nephritis.
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60. Alport Syndrome
Category Causes of Hearing Loss and Hearing Loss in General alport syndrome (Source Boystown Research Registry). alport syndrome
http://www.odc.state.or.us/tadoc/hloss2.htm
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Alport Syndrome
(Source: Boystown Research Registry) Alport Syndrome (AS) is characterized by hereditary nephritis (kidney disease known as Bright's disease in the past) and sensorineural hearing loss. The mode of inheritance may be X-linked or autosomal dominant. Less common symptoms include a defect of the lens of the eye called anterior lenticonus and a defect of blood platelets that can cause bleeding complications. AS is usually diagnosed by a test for blood and protein in the urine, hearing tests, and an extended family history. Hearing loss commonly occurs in childhood. Most subtypes of AS include a bilateral progressive sensorineural hearing loss of mild to moderate degree, but some individuals may have a severe to profound loss. Females generally have a milder hearing loss than their male relatives if they have one at all. Management of the hearing loss includes regular audiologic follow-up, use of hearing aides, and avoidance of certain drugs and excessive noise exposure that can cause further hearing loss. Mutations (changes from the normal genetic structure) responsible for AS have been found in a collagen gene, COL4A5, which is on the long arm of the X chromosome (Xq22). Several different mutations in the COL4A5 gene have been identified, which are thought to relate to the variation in age of onset and severity among families with AS. At this time a gene for autosomal dominant AS has not been identified.

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